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I7006

Sigma-Aldrich

Bis(3-aminopropyl)amine

Sinonimo/i:

3,3′-Diaminodipropylamine, 3,3′-Iminodipropylamine, N-(3-Aminopropyl)-1,3-propanediamine, Dipropylenetriamine, Norspermidine

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About This Item

Formula condensata:
(NH2CH2CH2CH2)2NH
Numero CAS:
56-18-8
Peso molecolare:
131.22
Beilstein:
1071254
Numero CE:
200-261-2
Numero MDL:
MFCD00008214
Codice UNSPSC:
12352100
ID PubChem:
24896102

Indice di rifrazione

n20/D 1.481 (lit.)

P. eboll.

151 °C/50 mmHg (lit.)

Punto di fusione

−14 °C (lit.)

Densità

0.938 g/mL at 25 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

NCCCNCCCN

InChI

1S/C6H17N3/c7-3-1-5-9-6-2-4-8/h9H,1-8H2
OTBHHUPVCYLGQO-UHFFFAOYSA-N

Informazioni sul gene

mouse ... Odc1(18263)

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Avvertenze

Danger

Indicazioni di pericolo

H302,H311,H314,H317,H330,H341,H373

Classi di pericolo

Acute Tox. 1 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Muta. 2 - Skin Corr. 1A - Skin Sens. 1A - STOT RE 2

Organi bersaglio

thymus

Codice della classe di stoccaggio

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

242.6 °F - closed cup

Punto d’infiammabilità (°C)

117 °C - closed cup

Dispositivi di protezione individuale

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

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Tris(2-aminoethyl)amine 96%

Sigma-Aldrich

225630

Tris(2-aminoethyl)amine

Tetraethylenepentamine technical grade

Sigma-Aldrich

T11509

Tetraethylenepentamine

Polyethylenimine, ethylenediamine end-capped average Mw ~800 by LS, average Mn ~600 by GPC

Sigma-Aldrich

408719

Polyethylenimine, ethylenediamine end-capped

Johannes Ghatnekar et al.
Bioorganic & medicinal chemistry, 15(23), 7426-7433 (2007-09-18)
We here report the synthesis of the two polyamine-based nucleoside derivatives 5-{[bis-(3-aminopropyl)amino]acetamido-1-propynyl}uridine and 2-{[bis-(3-aminopropyl)amino]-acetamido-1-propynyl}adenosine. The various polyamine derivatives have been used in thermal melting analysis using DNA from herring testes, and in cellular studies using four different cell lines. The
T Yorifuji et al.
Journal of biochemistry, 122(3), 537-543 (1997-11-05)
Polyamine aminotransferase of Arthrobacter sp. TMP-1 was induced by 1,3-diaminopropane (DAP), N-3-aminopropyl-1,3-diaminopropane (norspermidine), spermidine, and spermine, but not by putrescine. The enzyme was purified to homogeneity. Its molecular weight and subunit size were 129,000 and 64,000, respectively. Its absorption spectrum
T Shinki et al.
European journal of biochemistry, 183(2), 285-290 (1989-08-01)
We have reported that spermidine N1-acetyltransferase has a larger role than ornithine decarboxylase in putrescine synthesis in chick duodenum induced by 1 alpha,25-dihydroxycholecalciferol (calcitriol) [Shinki, T., Kadofuku, T., Sato, T. and Suda, T. (1986) J. Biol. Chem. 261, 11712-11716]. In
Ece Karatan et al.
Journal of bacteriology, 187(21), 7434-7443 (2005-10-21)
Vibrio cholerae is both an environmental bacterium and a human intestinal pathogen. The attachment of bacteria to surfaces in biofilms is thought to be an important feature of the survival of this bacterium both in the environment and within the
N J Prakash et al.
Anticancer research, 8(4), 563-568 (1988-07-01)
The structural specificities of the natural polyamines putrescine (Put), spermidine (Spd) and spermine (Spm) for cell growth are rather stringent, suggesting that appropriate structural analogues of these polycations could serve as potential antineoplastic agents via polyamine antagonism. Norspermidine (Nspd), a
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